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1.
PLoS One ; 18(10): e0288025, 2023.
Artículo en Inglés | MEDLINE | ID: mdl-37856438

RESUMEN

Human induced pluripotent stem cell (hiPSC)-derived brain spheroids can recapitulate the complex cytoarchitecture of the brain, as well as the genetic/epigenetic footprint of human brain development. However, hiPSC-derived 3D models such as spheroid and organoids does not have a perfusable microvascular network, which plays a vital role in maintaining homeostasis in vivo. With the critical balance of positive and negative angiogenic modulators, 3D microvascular network can be achieved by angiogenesis. This paper reports on a microfluidic-based three-dimensional, cortical spheroid grafted on the vascular-network. Vascular network was formed by inducing angiogenic sprouting using concentration gradient-driven angiogenic factors in the microfluidic device. We investigate critical factors for angiogenic vascular network formation with spheroid placement, including 1) a PKCα activator, phorbol-12-myristate-13-acetate (PMA); 2) orientation of endothelial cells under perfusion and permeability of vascular network; 3) effect of extracellular matrix (ECM) types and their densities on angiogenesis; and 4) integration with cortical spheroid on vascular network. This paper demonstrates proof of concept for the potential utility of a membrane-free in vitro cortical spheroid tissue construct with perfusable microvascular network that can be scaled up to a high throughput platform. It can provide a cost-effective alternative platform to animal testing by modeling brain diseases and disorders, and screening drugs.


Asunto(s)
Células Endoteliales , Células Madre Pluripotentes Inducidas , Animales , Humanos , Encéfalo , Microvasos , Dispositivos Laboratorio en un Chip , Esferoides Celulares
2.
Sci Rep ; 6: 38856, 2016 12 09.
Artículo en Inglés | MEDLINE | ID: mdl-27934939

RESUMEN

With great advances in the field of in vitro brain modelling, the challenge is now to implement these technologies for development and evaluation of new drug candidates. Here we demonstrate a method for culturing three-dimensional networks of spontaneously active neurons and supporting glial cells in a microfluidic platform. The high-throughput nature of the platform in combination with its compatibility with all standard laboratory equipment allows for parallel evaluation of compound effects.


Asunto(s)
Técnicas de Cultivo de Célula/instrumentación , Ensayos Analíticos de Alto Rendimiento/métodos , Dispositivos Laboratorio en un Chip , Células-Madre Neurales/citología , Neuroglía/efectos de los fármacos , Neuronas/efectos de los fármacos , Organoides/efectos de los fármacos , Potenciales de Acción , Forma de la Célula , Técnicas de Cocultivo , Colágeno , Combinación de Medicamentos , Humanos , Células Madre Pluripotentes Inducidas/citología , Laminina , Neuritas/ultraestructura , Neurogénesis , Neuroglía/citología , Neuronas/citología , Neurotoxinas/farmacología , Proteoglicanos
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